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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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38 records meeting your search criteria returned- Product Code: KKY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION HTR-PMI 1500889 RT FRT 10/04/2023
BIOMET MICROFIXATION HTR-PMI 646704 LF FRT PAR TEMP 02/21/2022
BIOMET MICROFIXATION HTR-PMI 990476 RT FRT TEMP PAR 10/27/2021
PORIFEROUS, LLC SU-POR SURGICAL IMPLANTS 09/17/2021
BIOMET MICROFIXATION HTR-PMI NE00-20 LF FRT TEM PAR 08/31/2021
BIOMET MICROFIXATION HTR-PMI NE00-20 LF FRT TEM PAR 08/31/2021
MATRIX SURGICAL USA OMNIPORE SURGICAL IMPLANT 08/27/2021
PORIFEROUS, LLC SU-POR SURGICAL IMPLANTS 06/21/2021
BIOMET MICROFIXATION HTR * PMI M.Y.1990 LEFT FRONTAL PARIETAL 02/01/2021
PORIFEROUS, LLC SU-POR SURGICAL IMPLANTS 10/23/2020
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